Renal effects of guideline-directed medical therapies in heart failure: a consensus document from the Heart Failure Association of the European Society of Cardiology.


Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
04 2022
Historique:
revised: 22 02 2022
received: 17 01 2022
accepted: 01 03 2022
pubmed: 4 3 2022
medline: 18 5 2022
entrez: 3 3 2022
Statut: ppublish

Résumé

Novel pharmacologic treatment options reduce mortality and morbidity in a cost-effective manner in patients with heart failure (HF). Undisputedly, the effective implementation of these agents is an essential element of good clinical practice, which is endorsed by the European Society of Cardiology (ESC) guidelines on acute and chronic HF. Yet, physicians struggle to implement these therapies as they have to balance the true and/or perceived risks versus their substantial benefits in clinical practice. Any worsening of biomarkers of renal function is often perceived as being disadvantageous and is in clinical practice one of the most common reasons for ineffective drug implementation. However, even in this context, they clearly reduce mortality and morbidity in HF with reduced ejection fraction (HFrEF) patients, even in patients with poor renal function. Furthermore these agents are also beneficial in HF with mildly reduced ejection fraction (HFmrEF) and sodium-glucose cotransporter 2 (SGLT2) inhibitors more recently demonstrated a beneficial effect in HF with preserved ejection fraction (HFpEF). The emerge of several new classes (angiotensin receptor-neprilysin inhibitor [ARNI], SGLT2 inhibitors, vericiguat, omecamtiv mecarbil) and the recommendation by the 2021 ESC guidelines for the diagnosis and treatment of acute and chronic HF of early initiation and titration of quadruple disease-modifying therapies (ARNI/angiotensin-converting enzyme inhibitor + beta-blocker + mineralocorticoid receptor antagonist and SGLT2 inhibitor) in HFrEF increases the likelihood of treatment-induced changes in renal function. This may be (incorrectly) perceived as deleterious, resulting in inertia of starting and uptitrating these lifesaving therapies. Therefore, the objective of this consensus document is to provide advice of the effect HF drugs on renal function.

Identifiants

pubmed: 35239201
doi: 10.1002/ejhf.2471
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Sodium-Glucose Transporter 2 Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

603-619

Informations de copyright

© 2022 European Society of Cardiology.

Références

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Auteurs

Wilfried Mullens (W)

Ziekenhuis Oost Limburg, Genk, University Hasselt, Hasselt, Belgium.

Pieter Martens (P)

Ziekenhuis Oost Limburg, Genk, University Hasselt, Hasselt, Belgium.
Cleveland Clinic, Cleveland, OH, USA.

Jeffrey M Testani (JM)

Yale University, New Haven, CT, USA.

W H Wilson Tang (WHW)

Cleveland Clinic, Cleveland, OH, USA.

Hadi Skouri (H)

American University of Beirut Medical Center-Beirut, Beirut, Lebanon.

Frederik H Verbrugge (FH)

Centre for Cardiovascular Diseases, University Hospital Brussel, Jette, Belgium.
Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, Brussels, Belgium.
Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium.

Marat Fudim (M)

Duke University Medical Center, Durham, NC, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Massimo Iacoviello (M)

Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy.

Jennifer Franke (J)

CardioVascular Center Frankfurt, Frankfurt, Germany.

Andreas J Flammer (AJ)

University Heart Center, University Hospital Zurich, Zurich, Switzerland.

Alberto Palazzuoli (A)

Cardiovascular Diseases Unit, Department of Medical Sciences, Le Scotte Hospital Siena, Siena, Italy.
School of Nursing and Midwifery, Queen's University, Belfast, UK.

Paola Morejon Barragan (PM)

Clinica Guayaquil, Guayaquil, Ecuador.

Thomas Thum (T)

Institute of Molecular and Translational Therapeutic Strategies (IMTTS), Hannover Medical School, Hannover, Germany.
Fraunhofer Institute of Toxicology and Experimental Medicine, Hannover, Germany.

Marta Cobo Marcos (MC)

Hospital Universitario Puerta de Hierro Majadahonda, CIBERCV, Madrid, Spain.

Òscar Miró (Ò)

Emergency Department, Hospital Clínic, Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.

Patrick Rossignol (P)

Université de Lorraine, Inserm 1433 CIC-P CHRU de Nancy, Inserm U1116, and F-CRIN INI-CRCT, Nancy, France.

Marco Metra (M)

University of Brescia, Brescia, Italy.

Johan Lassus (J)

Heart and Lung Center, Cardiology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Francesco Orso (F)

Università degli studi di Firenze, Florence, Italy.

Ewa A Jankowska (EA)

Institute of Heart Diseases, Wroclaw Medical University and Institute of Heart Diseases, University Hospital in Wroclaw, Wroclaw, Poland.

Ovidiu Chioncel (O)

Emergency Institute for Cardiovascular Diseases 'Prof. C.C. Iliescu', University of Medicine Carol Davila, Bucharest, Romania.

Davor Milicic (D)

Department of Cardiovascular Diseases, University of Zagreb School of Medicine & University Hospital Centre Zagreb, Zagreb, Croatia.

Loreena Hill (L)

School of Nursing & Midwifery, Queen's University, Belfast, UK.

Petar Seferovic (P)

Universi Faculty of Medicine, University of Belgrade, and Serbian Academy of Arts and Sciences, Belgrade, Serbia.

Giuseppe Rosano (G)

St George's University Medical School of London, London, UK.

Andrew Coats (A)

University of Warwick, Coventry, UK.

Kevin Damman (K)

University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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